化学
吸附
零价铁
傅里叶变换红外光谱
齿合度
电子顺磁共振
无机化学
氧化还原
电子转移
弗伦德利希方程
核化学
物理化学
金属
化学工程
有机化学
核磁共振
工程类
物理
作者
Fengfeng Zhou,Qiangling Liu,Yaxin Qin,Wei Liu,Lizhi Zhang
标识
DOI:10.1016/j.jhazmat.2023.131717
摘要
Herein, L-cysteine (Cys) was modified on zero-valent iron (C-ZVIbm) by using a mechanical ball-milling method to improve the surface functionality and the Cr(VI) removal efficiency. Characterization results indicated that Cys was modified on the surface of ZVI by the specific adsorption of Cys on the oxide shell to form a -COO-Fe complex. The Cr(VI) removal efficiency of C-ZVIbm (99.6%) was much higher than that of ZVIbm (7.3%) in 30 min. The attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) analysis inferred that Cr(VI) was more likely to be adsorbed on the surface of C-ZVIbm to form bidentate binuclear inner-sphere complexes. The adsorption process was well-matched to the Freundlich isotherm and the pseudo-second-order kinetic model. Electrochemical analysis and electron paramagnetic resonance (ESR) spectroscopy revealed that Cys on the C-ZVIbm lowered the redox potential of Fe(III)/Fe(II), and favored the surface Fe(III)/Fe(II) cycling mediated by the electrons from Fe0 core. These electron transfer processes were beneficial to the surface reduction of Cr(VI) to Cr(III). Our findings provide new understandings into the surface modification of ZVI with a low-molecular weight amino acid to promote in-situ Fe(III)/Fe(II) cycling, and have great potential for the construction of efficient systems for Cr(VI) removal.
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